HGVS | Genome Assembly |
---|---|
NC_000004.12:g.41745971del , CM000666.2:g.41745971del | GRCh38 |
NC_000004.11:g.41747988del , CM000666.1:g.41747988del | GRCh37 |
NC_000004.10:g.41442745del | NCBI36 |
NG_008243.1:g.8001del , LRG_513:g.8001del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226382.4:c.782del MANE Select | ENSP00000226382.2:p.Gly261GlufsTer? | |
ENST00000226382.3:c.782del | ENSP00000226382.2:p.Gly261GlufsTer? | |
NM_003924.3:c.782del , LRG_513t1:c.782del | NP_003915.2:p.Gly261GlufsTer? | |
NM_003924.4:c.782del MANE Select | NP_003915.2:p.Gly261GlufsTer? |